Livestock grazing in intermountain depressional wetlands—Effects on plant strategies, soil characteristics and biomass

https://doi.org/10.1016/j.agee.2013.04.017Get rights and content

Highlights

  • Livestock use influenced soil salinity, above- and belowground biomass, and plant CSR-strategy types in prairie wetlands.

  • Soil salinity increased and biomass was reduced by livestock use.

  • Competitors were less and ruderals more abundant in more intensely used wetlands.

  • Salinity only favored stress tolerators at low levels of use.

Abstract

Prairie wetlands are considered valuable habitat for plants, birds, and wildlife. Livestock use of these wetlands can create conflicts with conservation issues. To achieve proper management, patterns and processes induced by grazing livestock need to be understood. In this study, we examined interactions of livestock use, soil and vegetation of depressional prairie wetlands in British Columbia, Canada. Plant community composition, biomass, and soil properties (bulk density, salinity, nitrogen and carbon content) were sampled on transects in marsh and wet meadow vegetation zones of wetlands along a grazing intensity gradient. Grime's CSR-strategies were used to calibrate strategy signatures, which indicate the importance of competition, stress and disturbance. Heavily grazed sites had higher salinity, less biomass, and proportionally less belowground biomass. Differences concerning strategies between vegetation zones were only apparent in un/lightly grazed sites, where stress was higher in marsh and competition higher in wet meadow zones. Livestock use and nitrogen were positively correlated with ruderal abundance and negatively correlated with competitors and stress-tolerators. Livestock use was identified to be most influential on plant strategies. Our results indicate that heavy livestock use significantly alters vegetation patterns and processes in prairie wetlands and may have negative impact on valuable habitat. Management decisions should consider reduced livestock access and incorporate conservation issues in grazing schemes.

Introduction

Prairie wetlands and their associated vegetation play important ecological and economic roles in large parts of North America (Mitsch and Gosselink, 2000). As islands within relatively dry regions, they are especially vital for providing several ecological services, such as water filtration and storage (Leibowitz, 2003) and carbon sequestration (Euliss et al., 2006). They are fundamental in offering breeding habitat and shelter to a variety of waterfowl (Batt et al., 1989, Johnson et al., 2005), other wetland associated birds (Weller and Spatcher, 1965), and amphibians (Piha et al., 2007). Besides also hosting a number of wetland plant species, they supply wildlife with water and forage, and are thus of great conservation concern (Leibowitz, 2003, Seabloom and van der Valk, 2003). The semiarid grasslands, where these wetland ecosystems can be found, are important forage pastures for livestock and agriculture industries. Many of these wetlands have thus either been converted to agricultural land (Galatowitsch, 1993), or are under high grazing pressure by livestock (van Ryswyk et al., 1992).

Grazing is known to have the potential to alter ecosystems and change their structure and function (Hobbs, 1996). The general effects of livestock use on vegetation and soil are well-studied; cattle remove aboveground biomass, reduce litter accumulation, compact and disturb the soil (Austin et al., 2007, Greenwood and Mackenzie, 2001, Schulz and Leininger, 1990, Wheeler et al., 2002), further promoting erosion through mechanical disturbance of the soil surface (Pietola et al., 2005). Additionally, several studies have observed changed nutrient conditions (Bakker et al., 2004, Golluscio et al., 2009, McNaughton et al., 1997, Reeder and Schuman, 2002) and an increase in soil salinity (Belsky et al., 1999, Lavado and Taboada, 1987, Srivastava and Jefferies, 1996) under grazing in several regions. Moreover, a number of studies have investigated the responses of wetland vegetation communities to livestock use, and have found reactions to be dependent on hydrological conditions, and the intensity and seasonal occurrence of grazing (Austin et al., 2007, Jones et al., 2011, Lucas et al., 2004, Schulz and Leininger, 1990). Consistent findings regarding changes in vegetation and community structure show a decrease in litter accumulation, and shifts in plant functional types including decreased abundance of tall and rhizomatous species, and an increase of species with an annual lifecycle and short canopy height. On the other hand, moderate levels of disturbance have been shown to diversify vegetation composition and structure (e.g. Grace and Jutila, 1999, Marty, 2005, Jones et al., 2011), according to the ‘hump-backed model’ of plant species richness (Grime, 1973), and thus diversify habitats for other species (van Wieren, 1995, Metera et al., 2010). However, studies rarely consider the interactions of soil characteristics and livestock use and their relative importance in shaping vegetation patterns in prairie wetland vegetation.

One attempt to describe responses of plant communities to different soil and site characteristics has been made with Grime's plant strategy theory (Grime, 1974, Grime, 1977, Grime, 2001). This theory makes predictions about the distribution of species according to their adaptations to stress and disturbance, as well as their competitive ability when those two factors are negligible. Herein, stress is defined as a limitation of plant growth, either due to a deficit in essential resources or the presence of a growth-limiting factor, and disturbance as the destruction or damage of living plant material. Wetland vegetation is naturally exposed to stress through excess levels of water causing anoxic conditions. Livestock use has the potential to add to the stress component, by reducing nutrient availability and increasing salinity. Grazing and trampling, however, act as a disturbance (Grime, 2001), further altering competitive interactions (Gough and Grace, 1998). Species that are either tolerant or adapted to grazing (e.g. low palatability, adapted growth form) can react with compensatory growth, compensating or even increasing productivity (McNaughton, 1983), and are thus favored (Grime, 2001). Besides affecting plant growth, heavy grazing and trampling also creates gaps and reduces litter accumulation. This changes the competition for light (Olff and Ritchie, 1998), promoting the establishment of low growing perennial forbs and ruderal, early successional species (e.g. Bullock et al., 2001, Evju et al., 2010, Milchunas et al., 1988, van der Valk, 1986).

Depressional wetlands in the intermountain west are situated in a matrix of semiarid grasslands, similar to those in the Prairie Pothole Region of North America. But unlike the prairies east of the Rocky Mountains, this region did not support large herds of herbivores before human settlement and the introduction of cattle and horses (Mack and Thompson, 1982). Cattle ranching is now a widespread land use practice and of great commercial importance (van Ryswyk et al., 1992) making wetlands prone to alterations in their form and function. For this reason, it is essential to understand the processes, especially those altered by livestock use, to develop sustainable management practices for these valuable ecosystems.

This study examined the effects of livestock use on soil properties and plant strategies in depressional wetlands of southern interior British Columbia in the summer of 2010. We hypothesized that (i) soil salinity would increase, but soil carbon content, along with biomass and the proportion of belowground biomass, would decrease with increasing livestock use. We further expected (ii) stress-tolerant species to be more abundant in the more frequently inundated parts of the wetlands, and competitors to dominate drier and less disturbed areas. Additionally, we hypothesized that (iii) higher levels of salinity and decreased levels of nitrogen would increase the importance of stress tolerance, whereas high degrees of disturbance would primarily alter the vegetation community to more ruderal species, and decrease the importance of competition.

Section snippets

Study area

The study was conducted on the Thompson plateau in south central British Columbia, Canada (Fig. 1). This region is characterized by a continental semiarid climate, with mean annual precipitation of approximately 380 mm, and mean July temperature exceeding 20 °C at altitudes of the study sites (Wikeem and Wikeem, 2004).

Depressional wetlands in this area are similar in structure to those of the Prairie Pothole Region of North America (Kantrud, 1989), and are characterized by vegetation zones that

Soil properties and biomass

Soil pH ranged from moderately to strongly alkaline (pH 8.0–9.0), and samples showed no to moderate salinity (0.3–10.4 dS/m). Total carbon (C) and nitrogen (N) contents ranged from 4.2 to 23.6% and 0.33 to 1.85%, respectively. Topography of the sites, as measured by inclination, differed between livestock use categories (t-test: p < 0.001), heavily used sites being steeper (10.7 vs. 5.7%). Inclination showed correlations of moderate degree with bare ground (Spearman's ρ = −0.43, adj. p < 0.01), above-

Discussion

This study revealed the influence of livestock use on plant strategies, biomass, and selected physical and chemical soil properties in depressional prairie wetlands.

Most importantly, this study found a change in patterns of wetland vegetation caused by livestock grazing. The NMDS ordination showed that most variation in CSR-strategies occurred along the livestock use gradient. Differences between vegetation zones (i.e. hydrology and salinity) however, were only apparent at low grazing

Conclusions

Heavy grazing was found to strongly affect soils as well as vegetation in the studied wetlands. Natural processes in soils and vegetation communities were greatly disrupted by heavy livestock use. Soil salinity increased, and the disturbance by livestock predominantly influenced plant strategies.

Grazing in the study area has greatly increased since the introduction of cattle and horses, given that large herds of wild ungulates are believed to have been absent from this region west of the Rocky

Acknowledgements

We thank Amanda Schmidt, Justine McCulloch, Marc Jones, and Gesche Blume-Werry for assistance in the field and lab, and two anonymous reviewers for helpful comments on the manuscript. British Columbia Parks and The Nature Conservancy of Canada kindly granted access to their lands. LM Teuber was supported by a thesis scholarship of the German Academic Exchange Service (DAAD). Funding was provided by a Natural Sciences and Engineering Research Discovery Grant to LH Fraser.

References (58)

  • B.D.J. Batt et al.

    The use of prairie potholes by North American ducks

  • A.J. Belsky et al.

    Survey of livestock influences on stream and riparian ecosystems in the western United States

    J. Soil Water Conserv.

    (1999)
  • M.E. Biondini et al.

    Grazing intensity and ecosystem processes in a northern mixed-grass prairie, USA

    Ecol. Appl.

    (1998)
  • J.M. Bullock et al.

    A plant trait analysis of responses to grazing in a long-term experiment

    J. Appl. Ecol.

    (2001)
  • B.J. Cook et al.

    Effects of hydrologic connectivity on water chemistry, soils, and vegetation structure and function in an intermontane depressional wetland landscape

    Wetlands

    (2007)
  • J.G. Engels et al.

    Stress tolerance and biotic interactions determine plant zonation patterns in estuarine marshes during seedling emergence and early establishment

    J. Ecol.

    (2011)
  • M. Evju et al.

    Interactions between local climate and grazing determine the population dynamics of the small herb Viola biflora

    Oecologia

    (2010)
  • L.H. Fraser et al.

    Effect of minor water depth treatments in competitive effect and response of eight wetland plants

    Plant Ecol.

    (2008)
  • S. Galatowitsch

    Site Selection, Design Criteria and Performance Assessment for Wetland Restorations in the Prairie Pothole Region

    (1993)
  • R.A. Golluscio et al.

    Sheep grazing decreases organic carbon and nitrogen pools in the Patagonian steppe: combination of direct and indirect effects

    Ecosystems

    (2009)
  • L. Gough et al.

    Herbivore effects on plant species density at varying productivity levels

    Ecology

    (1998)
  • J.B. Grace et al.

    The relationship between species density and community biomass in grazed and ungrazed coastal meadows

    Oikos

    (1999)
  • K.L. Greenwood et al.

    Grazing effects in soil physical properties and the consequences for pastures: a review

    Aust. J. Exp. Agric.

    (2001)
  • J.P. Grime

    Competitive exclusion in herbaceous vegetation

    Nature

    (1973)
  • J.P. Grime

    Vegetation classification by reference to strategies

    Nature

    (1974)
  • J.P. Grime

    Evidence for the existence of three primary strategies in plants and its relevance to ecological and evolutionary theory

    Am. Nat.

    (1977)
  • J.P. Grime

    The ecology of species, families and communities of the contemporary British flora

    New Phytol.

    (1984)
  • J.P. Grime

    Plant Strategies, Vegetation Processes, and Ecosystem Properties

    (2001)
  • J.P. Grime et al.

    Comparative Plant Ecology—A Functional Approach to Common British Species

    (2007)
  • Cited by (24)

    • Debris Barriers Reduce the Effects of Livestock Grazing Along Streams After Timber Harvest

      2022, Rangeland Ecology and Management
      Citation Excerpt :

      Litter can influence the understory microclimate due to its modulation of soil temperature and moisture; thus, litter accumulation can be viewed as a positive effect of grazing exclusion by debris barriers (Dormaar et al. 1997; Jacobo et al. 2006). Barriers only significantly reduced bare soil compared with controls, in the Echo site, contrary to studies that show consistent increases in ground cover with increased grazing (Yeo 2005; Teuber et al. 2013; Goosey et al. 2019; Valdez-Cepeda et al. 2021), although Ferreira et al. (2020) did not observe exclosure effects after the first year of a 4-yr experiment. The lack of a treatment effect in three sites could be a result of inadequate grazing pressure.

    • Grazing Effects on the Composition, Diversity, and Function of Wet Meadow Grasslands in Manitoba, Canada

      2022, Rangeland Ecology and Management
      Citation Excerpt :

      These questions remain an important gap in understanding the effect of grazing on wet meadow grasslands and are the focus of ongoing research. Although we did not measure the traits of dominant plants (e.g., Janeček et al. 2013; Májeková, et al. 2016) or categorize dominant plants based on their functional strategies (e.g., Teuber et al. 2013), these approaches, including those that focus on belowground plant traits, promise important insights into the effects of grazing on the structure and function of wet meadows and remain an important focus for future research. For example, a community shift toward grasses following early grazing could create a community more resistant to flooding (Teuber et al. 2013).

    • Degradation shifts plant communities from S- to R-strategy in an alpine meadow, Tibetan Plateau

      2021, Science of the Total Environment
      Citation Excerpt :

      Since then, CSR theory has been widely applied to examine and interpret community processes, such as the variations of species diversity (Cerabolini et al., 2010), community stability and succession (Caccianiga et al., 2006). Thus, numerous experiments have been conducted to characterize, map and compare plants' CSR strategies for forests (Rosenfield et al., 2019), rangelands (Negreiros et al., 2014) and wetlands (Teuber et al., 2013) under different habitats. Although different strategies were detected in worldwide forests (Rosenfield et al., 2019; Silva et al., 2018), S-selected species dominate in various rangelands, e.g. tropical grasslands (Matos et al., 2021), temperate grasslands (Busch et al., 2019) and alpine rangeland (Pierce et al., 2007) with stressful environments (Caccianiga et al., 2006; Pierce et al., 2007).

    • Rotation grazing as a conservation management tool: Vegetation changes after six years of application in a salt marsh ecosystem

      2017, Agriculture, Ecosystems and Environment
      Citation Excerpt :

      Grazing in moderate densities generally improves plant diversity and vegetation dynamics (incl. recruitment) in productive (non-arid) systems, mainly via selective feeding, trampling and dung deposition (Bakker et al., 2006; Milchunas et al., 1988). However, grazing in high densities may lead to biodiversity loss, through the reduction in vegetation biomass, structure, and disturbance (Evans et al., 2015; Nolte et al., 2014; Teuber et al., 2013). Furthermore, different grazing regimes (i.e. varying in densities and species) have differential impact on the various taxa (van Klink et al., 2016).

    • Managing for species composition or diversity? Pastoral and free grazing systems in alkali steppes

      2016, Agriculture, Ecosystems and Environment
      Citation Excerpt :

      However, case studies on grazing effects of robust cattle breeds on pasture vegetation are rather scarce (but see Mann and Tischew, 2010; Török et al., 2014; Gilhaus et al., 2014; Cornelissen and Vulink, 2015). Beyond the analysis of the specific changes in cover and taxonomic diversity a more functional approach became increasingly involved in analyzing the usefulness of biodiversity conservation and restoration measures (Teuber et al., 2013; Kechang et al., 2015; Komac et al., 2015). A trait-based approach by studying the various components of functional diversity may reveal mechanisms how management influences both biodiversity and related ecosystem functioning (Carmona et al., 2012).

    View all citing articles on Scopus
    View full text